Collects and organizes patient data Maintains records and databases Uses software programs to generate graphs and reports Assists with recruiting patients for clinical trials Obtains patient study data from medical records, physicians, etc. Conducts literature searches Verifies accuracy of study forms Updates study forms per protocol Documents patient visits and procedure

Our PAs work under the supervision and direction of our supervising physicians to ensure high quality, safe and timely care for patients with various chief complaints. The PA team manages very sick patients, handles various high acuity procedures, and performs medical screening examinations in order to stabilize and treat those seeking services from the Emergency Room. Th

Works with Precision Medicine Strategy Lead as well as clinical study teams to ensure quality samples and data are delivered to support biomarker evaluation and delivery of science to medicine. Responsibilities include oversight of clinical sample collection, usage per informed consent form, sample tracking (chain of custody) and sample destruction. Individual will work c

Utilize MS Access, Excel and REDCap to assist in data collection efforts, database development, and descriptive data analysis. (In house REDCap and MS Access training is available.) Assist with preparation of Institutional Review Board(IRB) documentation and forms for study protocol approvals and amendments. Schedule conference calls; prepare agendas and pre meeting mater

The Study Coordinator is responsible for on and off site study implementation and data management of clinical research studies at both domestic (Boston) and international (South Africa) sites. Responsible for development and oversight of study documentation (i.e., protocols, data management and clinical quality management plans, standard operating procedures, informed con

Assist PI in development of protocol specific tools to aid in study documentation Assess eligibility of research subjects in accordance with the approved protocol and all applicable regulations including HIPAA Obtain patient consent and Human Subject Committee approvals for minimal risk studies as delegated by IRB approved protocol Collect, record, evaluate, update, and s

Pre & Post Award Research Administrator Job ID 2024 2325 Category Administrative Type regular Location Location US MA Woods Hole Job Summary Woods Hole Oceanographic Institution (WHOI) is seeking a Pre and Post Award Administrator to work in the Physical Oceanography (PO) Department. This is a regular, full time, exempt position, and is eligible for full benefits. The Adm

Data entry of test orders, presort, pickup and delivery of processed specimens to the laboratory, centrifugation and aliquoting Process specimens to be sent out to additional facilities Prepare laboratory specimens for various analysis and testing Identifies problems and in some cases, may resolve issues with specimen types such as missing information etc. Understands the

Under the guidance of the Principal Investigator (PI) or their appointed delegate, the role of Clinical Research Coordinator entails the independent execution of tasks and procedures associated with human subject research. This responsibility encompasses the coordination of regulatory components management and compilation of data pertaining to multifaceted research protoc

Implementation of research protocols with the program manager and research support team, including 1) remote surveys and clinical assessments; 2) clinical, cognitive, and biomarker based assessments in the first years of life; 3) biospecimen collection during pregnancy and childbirth; 4) virtual focus groups involving providers, patients, and community stakeholders; and 5

Under the direction of the Central Team Leader and Manager for Clinical Services, ensures optimum patient outcomes related to medication use by preventing or resolving drug related problems and coordinating the acquisition, distribution and control of all drug therapy to patients under the care of the pharmacist. Position Clinical Pharmacist Department Inpatient Pharmacy

Collects and organizes patient data Maintains records and databases Uses software programs to generate graphs and reports Recruiting patients for clinical trials, conducts phone interviews and schedules patients for visits. Obtains patient study data from medical records, physicians, etc. Conducts library searches Performs administrative support duties as required Verifie

Seeking a Pharmacy Technician Team Lead for a full time position with benefits. Ideal schedule 6 30 AM 3 00 PM or 7 00 AM 3 30 PM, Monday to Friday, within operation hours of 6 00 AM 9 30 PM. Sign On Bonus available. Job Description Under the direction of the Director of Pharmacy, the Pharmacy Technician Team Lead supervises the day to day activities of Certified Pharmacy

UMass Boston invites applications for a clinical lecturer who will hold a full time 12 month non tenure track faculty position in the Department of Nursing. Our programs focus on health in urban populations of all ages and target improving health equity in populations at risk for healthcare disparities. For more information go to www.umb.edu/academics/cnhs The position is

As a Pharmacy Technician, you wear a couple different hats throughout the course of the day, each one playing a significant role in the success of the department. Whether you are filling prescriptions, assisting a customer, or supporting other pharmacy team members, we count on you to deliver an unparalleled customer experience with a high level of professionalism, confid